CLASS II ONGOING Device recall · Reported 30 Mar 2022 · FDA Enforcement Report
Medical Device products purchased from Family Dollar retail recalled
Dollar Tree Distribution is recalling Medical Device products purchased from Family Dollar retail stores located in Alabama, distributed nationwide in the US. The recall was initiated on 18 Feb 2022 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0822-2022
- FDA event ID
- 89658
- Recalling firm
- Dollar Tree Distribution, Chesapeake, VA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 18 Feb 2022
- FDA classified
- 23 Mar 2022
- Reported
- 30 Mar 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Foreign Material
- Device type
- Surgical Instruments
Timeline
| 18 Feb 2022 | Recall initiated by company | |
| 23 Mar 2022 | Classified by FDA | +33 days |
| 30 Mar 2022 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential exposure to rodents and rodent activity in the distribution center.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee. The general categories of products, but are limited to these products, includes: feminine hygiene products, surgical masks, contact lens cleaning solutions, bandages, nasal care products
Where it was distributed
US Nationwide distribution: Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee O.U.S.: N/A
Nationwide AlabamaArkansasLouisianaMissouriMississippiTennessee
Stores named: Dollar Tree
Questions about this recall
Why was it recalled?
Potential exposure to rodents and rodent activity in the distribution center.
Which lots are affected?
All medical device products purchased from Family Dollar retail stores located in AL, AR, LA, MS, MO, and TN from January 1, 2021 to present.
Where was it sold?
US Nationwide distribution: Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee O.U.S.: N/A
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Dollar Tree Distribution
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Certain Over-The-Counter recalled by Dollar Tree Distribution | Dollar Tree Distribution | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | All Over-The-Counter recalled by Dollar Tree Distribution | Dollar Tree Distribution | Foreign Material | 6 states |
| Food | CLASS II | Food products purchased from Family Dollar retail stores recalled | Dollar Tree Distribution | Foreign Material | 6 states |
| Food | CLASS II | Dietary supplements purchased from Family Dollar retail recalled | Dollar Tree Distribution | Foreign Material | 6 states |
| Food | CLASS II | Candy Canes, Peppermint Flavor recalled by Dollar Tree Distribution | Dollar Tree Distribution | Foreign Material | Nationwide |
Other Surgical Instruments recalls
All 3,883| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Hopkins Telescope 30¿ recalled by Karl Storz Endoscopy | Karl Storz Endoscopy | Packaging Defects | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 24" X 4" 1-Line, Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 15" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 1-Line (CS Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 44" X 4" 2-Line, Green recalled | ASP Global | Device Malfunction | Nationwide |